Guo Guoxiao, He Zhikuan, Shi Zhaohui
Department of General Surgery, Henan University Huaihe Hospital, Kaifeng, Henan 475000, P.R. China.
Oncol Lett. 2016 Aug;12(2):1554-1558. doi: 10.3892/ol.2016.4752. Epub 2016 Jun 17.
The aim of the present study was to investigate the expression and function of forkhead box protein 3 (FOXP3) in gastric cancer using a rat model. A total of 92 Wistar rats were divided into two groups: An experimental group (n=46) and a control group (n=46). In the experimental group, sarcosine ethyl ester hydrochloride and sodium nitrite carcinogens were administered for 6 months to induce gastric cancer, whereas the control group was administered saline. Reverse transcription-polymerase chain reaction, immunoblotting, immunohistochemistry and western blotting were applied to analyze FOXP3 expression in gastric cancer and normal gastric tissue in the experimental and control groups, respectively. The association between FOXP3 expression and gastric cancer pathogenesis was investigated. In the experimental group, 6/46 rats developed hyperplastic lesions (grade I), 8 rats developed precancerous lesions (grade II), 18 rats developed early stage gastric cancer (grade III) and 14 rats developed gastrointestinal invasive carcinoma (grade IV). FOXP3 transcription and expression was observed in all gastric tissues of the experimental group. FOXP3 transcription and expression levels were significantly higher in the experimental group than in the control group (P<0.05). Furthermore, in the experimental group, a higher lesion grade was associated with a higher level of FOXP3 transcription and expression (P<0.05). FOXP3 protein was predominantly distributed in the tumor nuclei of the gastric cancer tissues. In the 32 pathological slices of gastric cancer tissue obtained from the experimental group, 20 cases (62.50%) exhibited positive FOXP3 staining. In the hyperplastic (grade I) and precancerous gastric (grade II) tissues, 2 cases (33.33%) and 4 cases (50.00%) exhibited positive FOXP3 staining, respectively. However, no positive FOXP3 expression was identified in the 46 pathological gastric tissue slices obtained from the control group. In conclusion, the expression of FOXP3 exhibits a positive correlation with gastric lesion grade. Therefore, FOXP3 may exhibit an important function in the occurrence and development of gastric cancer.
本研究旨在利用大鼠模型探讨叉头框蛋白3(FOXP3)在胃癌中的表达及功能。将92只Wistar大鼠分为两组:实验组(n = 46)和对照组(n = 46)。实验组给予肌氨酸乙酯盐酸盐和亚硝酸钠致癌物6个月以诱导胃癌,而对照组给予生理盐水。分别应用逆转录-聚合酶链反应、免疫印迹、免疫组织化学和蛋白质印迹分析实验组和对照组胃癌组织及正常胃组织中FOXP3的表达。研究FOXP3表达与胃癌发病机制之间的关联。实验组中,6/46只大鼠出现增生性病变(I级),8只大鼠出现癌前病变(II级),18只大鼠出现早期胃癌(III级),14只大鼠出现胃肠道浸润癌(IV级)。在实验组所有胃组织中均观察到FOXP3转录和表达。实验组中FOXP3转录和表达水平显著高于对照组(P<0.05)。此外,在实验组中,病变级别越高,FOXP3转录和表达水平越高(P<0.05)。FOXP3蛋白主要分布于胃癌组织的肿瘤细胞核中。在实验组获得的32例胃癌组织病理切片中,20例(62.50%)FOXP3染色呈阳性。在增生性(I级)和癌前胃(II级)组织中,分别有2例(33.33%)和4例(50.00%)FOXP3染色呈阳性。然而,在对照组获得的46例胃组织病理切片中未发现FOXP3阳性表达。总之,FOXP3的表达与胃病变级别呈正相关。因此,FOXP3可能在胃癌的发生发展中发挥重要作用。